| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:134253298-134253584 | Common:2; Rare:93; Clinvar (benign):1 | ||||
| chr12:389249-389360 | Rare:39 | ||||
| chr12:2004439-2004666 | Common:2; Rare:67 | ||||
| chr12:2877031-2877260 | Rare:69 | ||||
| chr12:3077280-3077428 | Common:4; Rare:67 | ||||
| chr12:3873355-3873563 | Common:2; Rare:46 | ||||
| chr12:4320949-4321258 | Common:5; Rare:117 | ||||
| chr12:4538431-4538795 | Rare:76 | ||||
| chr12:4649026-4649143 | Common:1; Rare:40; Clinvar (benign):1 | ||||
| chr12:6383970-6384268 | Common:1; Rare:72 | ||||
| chr12:6452087-6452119 | Rare:8 | ||||
| chr12:6493230-6493386 | Common:6; Rare:44 | ||||
| chr12:6493785-6494142 | Common:2; Rare:108 | ||||
| chr12:6534232-6534602 | Common:6; Rare:142 | ||||
| chr12:6568249-6568425 | Rare:67 |